EP0368198B1 - Thermoplastische Formmasse und Verfahren zu deren Herstellung - Google Patents

Thermoplastische Formmasse und Verfahren zu deren Herstellung Download PDF

Info

Publication number
EP0368198B1
EP0368198B1 EP89120488A EP89120488A EP0368198B1 EP 0368198 B1 EP0368198 B1 EP 0368198B1 EP 89120488 A EP89120488 A EP 89120488A EP 89120488 A EP89120488 A EP 89120488A EP 0368198 B1 EP0368198 B1 EP 0368198B1
Authority
EP
European Patent Office
Prior art keywords
percent
molding composition
thermoplastic molding
carbon monoxide
copolymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP89120488A
Other languages
English (en)
French (fr)
Other versions
EP0368198A2 (de
EP0368198A3 (de
Inventor
Hani Farah
Chai Jing Chou
Don R. Roden, Jr.
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Publication of EP0368198A2 publication Critical patent/EP0368198A2/de
Publication of EP0368198A3 publication Critical patent/EP0368198A3/de
Application granted granted Critical
Publication of EP0368198B1 publication Critical patent/EP0368198B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L73/00—Compositions of macromolecular compounds obtained by reactions forming a linkage containing oxygen or oxygen and carbon in the main chain, not provided for in groups C08L59/00 - C08L71/00; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers

Definitions

  • This invention relates generally to thermoplastic molding compositions comprising polycarbonates and, more particularly, to environmental stress failure resistant and impact resistant polymer blends comprising a polycarbonate, a polyester and a copolymer of ethylene and carbon monoxide.
  • Polycarbonates are well-known commercially available resinous materials having a variety of applications. They are typically prepared by the reaction of dihydroxy compounds with a carbonate precursor, such as phosgene, in the presence of a catalyst. Methods of direct phosgenation, interfacial condensation and transesterification, for the preparation of polycarbonates, are described in detail in "The Chemistry and Physics of Polycarbonates", by H. Schnell, John Wiley & Co., N.Y., 1964.
  • Polycarbonates are high temperature, high performance engineering thermoplastics having a combination of good thermal and mechanical properties, especially when prepared from one or more aromatic diols.
  • the blending with polycarbonates of additional compounds such as, for example, other thermoplastic resins and copolymer rubber compounds is commonly practiced in order to improve one or more properties of the homopolymer polycarbonate.
  • U.S. Patent No. 3,431,224 discloses a blend of a polycarbonate and a polyolefin such as polyethylene or an olefin copolymer such as ethylene/propylene, in order to improve the environmental stress failure resistance of the homopolycarbonate.
  • U.S. Patent No. 4,180,494 discloses the use of a butadiene-based core-shell copolymer for improving the environmental stress failure resistance of a blend of polycarbonate and polyester resins.
  • U.S. Patent No. 4,476,274 discloses polyethylene and glass fibers for improved impact resistance
  • U.S. Patents Nos. 3,780,139 and 4,271,063 disclose a terpolymer of ethylene, carbon monoxide and a third component such as vinyl acetate for improved strength
  • U.S. Patent No. 4,639,481 discloses polyethylene or a polyolefin copolymer for improved impact resistance.
  • the present invention is directed toward a novel polymer blend, comprising an aromatic polycarbonate, an aromatic polyester, and a copolymer of ethylene and carbon monoxide.
  • the blend surprisingly is highly impact resistant, and is likewise resistant to environmental stress failure.
  • the polymer blends of the present invention exhibit high impact resistance, chemical resistance, temperature stability, and excellent thermoplastic engineering properties, making them particularly suitable for producing molded plastic components for the automotive and electrical housing manufacturing industries.
  • aromatic polycarbonates suitable for use in the present invention are produced by any of the conventional processes known in the art for the manufacture of polycarbonates.
  • aromatic polycarbonates are prepared by reacting an aromatic dihydric phenol with a carbonate precursor, such as for example phosgene, a haloformate or a carbonate ester.
  • a preferred method for preparing the aromatic polycarbonates suitable for use in the present invention involves the use of a carbonyl halide, such as phosgene, as the carbonate precursor.
  • This method involves passing phosgene gas into a reaction mixture containing an activated dihydric phenol, or a nonactivated dihydric phenol and an acid acceptor such as, for example pyridine, dimethyl aniline and quinoline.
  • the acid acceptor may be used undiluted or diluted with inert organic solvents, such as methylene chloride, chlorobenzene or 1,2-dichloroethane.
  • Tertiary amines are advantageous since they are good solvents as well as acid acceptors during the reaction.
  • the temperature at which the carbonyl halide reaction proceeds may vary from below 0°C to 100°C.
  • the reaction proceeds satisfactorily at temperatures from room temperature to 50°C. Since the reaction is exothermic, the rate of phosgene addition may be used to control the temperature of the reaction.
  • the amount of phosgene required will generally depend upon the amount of dihydric phenols present. Generally speaking, one mole of phosgene will react with one mole of dihydric phenol to form the polycarbonate and two moles of HCl. The HCl is in turn taken up by the acid acceptor.
  • Another method for preparing the aromatic polycarbonates useful in the present invention comprises adding phosgene to an alkaline aqueous suspension of dihydric phenols. This is preferably done in the presence of inert solvents such as, for example, methylene chloride and 1,2-dichloroethane. Quaternary ammonium compounds may be employed to catalyze the reaction.
  • Yet another method for preparing such aromatic polycarbonates involves the phosgenation of an agitated suspension of an anhydrous alkali salt of an aryl diol in a nonaqueous medium such as benzene, chlorobenzene or toluene.
  • the reaction is illustrated by the addition of phosgene to a slurry of the sodium salt of, for example, Bisphenol A in an inert polymer solvent such as chlorobenzene.
  • a haloformate such as the bis-haloformate of Bisphenol A may be used in place of phosgene as the carbonate precursor in any of the methods described above.
  • ester interchange occurs between the carbonate ester and the dihydric phenol used.
  • the ester interchange is advantageously consummated at reduced pressures on the order of from (10 to 100 millimeters of mercury) 1.3 to 13 kPa, preferably in an inert atmosphere such as nitrogen or argon.
  • the polymer forming reaction may be conducted in the absence of a catalyst, one may, if desired, employ a typical ester exchange catalyst, such as metallic lithium, potassium, calcium or magnesium.
  • a typical ester exchange catalyst such as metallic lithium, potassium, calcium or magnesium.
  • the amount of such catalyst, if used, is usually small, ranging from 0.001 percent to 0.1 percent, based on the weight of the dihydric phenols employed.
  • the aromatic polycarbonate emerges from the reaction in either a true or pseudo solution depending on whether an aqueous base or pyridine is used as an acid acceptor.
  • the copolymer may be precipitated from the solution by adding a polymer nonsolvent, such as heptane or isopropanol.
  • the polymer solution may be heated, typically under reduced pressure, to evaporate the solvent.
  • a preferred aromatic polycarbonate is characterized by repeated units corresponding to the general formula: wherein X is a divalent C1-C15 hydrocarbon radical, a single bond, -O-, -S-, -S2-, -SO-, -SO2-, or -CO-. Each aromatic ring may additionally contain 1 or 2 substituents such as C1-C4 alkyl hydrocarbon radicals or halo radicals.
  • a most preferred aromatic polycarbonate is prepared form 2,2-bis-(4-hydroxyphenyl)-propane (Bisphenol A).
  • aromatic polycarbonate are the polycarbonate/polyester copolymers of the types disclosed in U.S. Patents Nos. 3,169,121, 4,105,633, 4,156,069, 4,260,731 and 4,287,787, as well as mixtures of polycarbonates and polycarbonate/polyester copolymers.
  • aromatic polyesters suitable for use according to the present invention may be generally prepared by condensing aromatic dicarboxylic acids with diols, or by condensing precursors which contain both an alcohol or phenol and a carboxylic acid.
  • Suitable aromatic dicarboxylic acids include, for example, terephthalic acid, isophthalic acid, naphthalene-dicarboxylic acid, diphenyletherdicarboxylic acid, diphenyldicarboxylic acid, diphenylsulfonedicarboxylic acid and diphenoxyethanedicarboxylic acid.
  • aromatic diols examples include hydroquinone, resorcinol, 2,2-bis-(4-hydroxyphenyl)propane, bis-(4-hydroxyphenyl)methane, 4,4′-thiodiphenol, bis-(4-hydroxyphenyl)sulfone, 4,4′-oxydiphenyl, 4,4′-dihydroxybiphenyl, and dihydroxynaphthalenes.
  • the aliphatic diols suitable for preparation of the aromatic polyesters include, for example, ethylene glycol, 1,3-propylene glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol and cyclohexane dimethylol.
  • precursors which contain both an alcohol and a carboxylic acid are 4-hydroxybenzoic acid and 2-hydroxy-6-naphthoic acid.
  • Polyesters may be prepared using any of the several well known methods such as, for example, by the reaction of the acid chloride of a carboxylic acid with an alcohol or phenol in the presence of a base; dehydration of an acid and alcohol or phenol through physical or chemical means; reaction of the ester derivative of a carboxylic acid (such as a methyl or phenyl ester) with an alcohol or phenol; or reaction of a carboxylic acid with a derivative (such as an acetate) of an alcohol or phenol.
  • Contemplated equivalent polyesters having the same operability and utility, may contain for example the following repeated mer units:
  • polyester as used in the present invention, is also contemplated copolyesters, which may be prepared by cocondensing one or more aromatic dicarboxylic acids with one or more diols.
  • liquid crystalline polyesters derived from mixtures of 4-hydroxybenzoic acid and 2-hydroxy-6-naphthoic acid; or mixtures of terephthalic acid, 4-hydroxybenzoic and ethylene glycol; or mixtures of terephthalic acid, 4-hydrobenzoic acid, and 4,4′-dihydroxybiphenyl.
  • a preferred polyester is characterized by repeated units corresponding to the general formula: wherein n is selected from the numbers 2 through 6.
  • a most preferred aromatic polyester is polyethylene terephthalate.
  • the ethylene/carbon monoxide copolymers of the present invention may be prepared by polymerizing ethylene with carbon monoxide, at an elevated temperature and pressure, in the presence of a catalyst such as a peroxy compound or azo compound. Specific procedures for preparing the copolymers are more fully set forth in U.S. Patents Nos. 2,495,285, 2,541,987, 4,024,325 and 4,024,326.
  • the amount of carbon monoxide in the copolymer is from 0.1 percent to 50 percent of the total weight of the copolymer; preferably it is from 2 percent to 15 percent by weight.
  • the polymer blend of the present invention comprises from 5 percent to 95 percent, preferably from 40 percent to 85 percent, of an aromatic polycarbonate; from 60 percent to 2 percent, preferably from 40 percent to 3 percent, of an aromatic polyester; and from 0.1 to 40 percent, preferably 1 percent to 25 percent, most preferably from 2 percent to 15 percent, of an ethylene/carbon monoxide copolymer.
  • the recited percentages are in relation to the total weight of the resinous blend.
  • the components may be mixed in any order, by the use of any conventional mixing apparatus.
  • polystyrene copolymers may obviously contain additional elastomeric impact modifiers such as, for example, acrylonitrile-butadiene-styrene copolymers (ABS copolymers), methylmethacrylate-butadiene-styrene copolymers (MBS rubbers), hydrogenated styrene-butadiene copolymers, functionalized EPDM copolymers, acrylic latexes, polybutadiene, polyisoprene and polybutene.
  • ABS copolymers acrylonitrile-butadiene-styrene copolymers
  • MVS rubbers methylmethacrylate-butadiene-styrene copolymers
  • EPDM copolymers functionalized EPDM copolymers
  • these impact modifiers are better tougheners for polycarbonate/polyester blends containing the ethylene/carbon monoxide copolymer than for the same polycarbonate/polyester blends containing known polyolefins such as, for example, polyethylene.
  • the polymer blends of the present invention may furthermore contain conventional thermoplastic polymer additives such as, for example, fillers, thermal stabilizers, dyes, flame retarding agents, reinforcing agents, softeners, mold-release agents, seed-forming agents, pigments, plasticizers, antistatic agents, ultraviolet radiation absorbers and lubricants, in conventional amounts generally not exceeding 50 percent of the total weight.
  • conventional thermoplastic polymer additives such as, for example, fillers, thermal stabilizers, dyes, flame retarding agents, reinforcing agents, softeners, mold-release agents, seed-forming agents, pigments, plasticizers, antistatic agents, ultraviolet radiation absorbers and lubricants, in conventional amounts generally not exceeding 50 percent of the total weight.
  • Dry blends comprising polycarbonate and polyester resins and ethylene/carbon monoxide copolymer were prepared in the proportions described in Table I (as were comparison compositions), and subsequently melt-mixed in a co-rotating twin screw extruder.
  • the resulting polymer blend strands were quenched and pelletized, and the pellets injection molded into test specimens whose mechanical properties are described in Tables II and III.
  • the percent elongation at break values for polymer compositions containing the copolymer of ethylene and carbon monoxide were superior to those for corresponding formulations utilizing polyethylene.
  • the retention of properties after treatment in a synthetic gasoline was reasonable up to about 15 percent polyester content. More delamination was observed for blends containing polyethylene than those containing the ethylene/carbon monoxide copolymer.
  • the impact modifier was surprisingly a more efficient toughener for the blends containing the ethylene/carbon monoxide copolymer than for blends containing polyethylene, as demonstrated by the notched Izod impact and falling dart impact results.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Claims (10)

  1. Thermoplastische Formmasse, umfassend, bezogen auf das Gesamtgewicht der Harzmischung,:
    A. von 5 bis 95 % eines aromatischen Polycarbonates;
    B. von 60 bis 2 % eines aromatischen Polyesters;
    C. von 0,1 bis 40 % eines Copolymeren von Ethylen und Kohlenmonoxid, wobei dieses Copolymere keines ist, das von Ethylen, Kohlenmonoxid und einem oder mehreren Termonomeren abstammt, und das von 0,1 bis 50 Gew.-% Kohlenmonoxid umfaßt.
  2. Thermoplastische Formmasse nach Anspruch 1, worin das aromatische Polycarbonat durch sich wiederholende Einheiten gekennzeichnet ist, die der allgemeinen Formel entsprechen :
    Figure imgb0009
     worin X ein zweiwertiger C₁-C₁₅-Kohlenwasserstoffrest, eine Einfachbindung, -O-, -S-, -S₂-, -SO-, -SO₂- oder -CO- ist, und worin weiterhin jeder aromatische Ring wahlweise 1 oder 2 C₁-C₄-Alkylkohlenwasserstoffrest- oder Halogenrest-Substituenten enthalten kann.
  3. Thermoplastische Formmasse nach Anspruch 2, worin das aromatische Polycarbonat aus Bisphenol A hergestellt ist.
  4. Thermoplastische Formmasse nach Anspruch 1, worin der aromatische Polyester durch sich wiederholende Einheiten gekennzeichnet ist, die der allgemeinen Formel entsprechen :
    Figure imgb0010
     worin n aus den Zahlen 2 bis 6 ausgewählt ist.
  5. Thermoplastische Formmasse nach Anspruch 4, worin der aromatische Polyester Polyethylenterephthalat ist.
  6. Thermoplastische Formmasse nach Anspruch 1, worin das Copolymere von Ethylen und Kohlenmonoxid von 2 Gew.-% bis 15 Gew.-% Kohlenmonoxid umfaßt.
  7. Thermoplastische Formmasse nach Anspruch 6, welche von 40 % bis 85 % an aromatischem Polycarbonat, bezogen auf das Gesamtgewicht der Polymere, umfaßt.
  8. Thermoplastische Formmasse nach Anspruch 7, welche von 40 % bis 3 % an aromatischem Polyester, bezogen auf das Gesamtgewicht der Polymere, und von 0,1 % bis 40 % eines Copolymeren von Ethylen und Kohlenmonoxid, bezogen auf das Gesamtgewicht der Polymere, umfaßt.
  9. Thermoplastische Formmasse nach Anspruch 1, weiterhin umfassend ein elastomeres Schlagzähigkeitsmodifikationsmittel, ausgewählt aus Acrylnitril-Butadien-Styrolcopolymeren, Methylmethacrylat-Butadien-Styrolcopolymenren, hydrierten Styrol-Butadiencopolymeren, funktionalisierten EPDM-Copolymeren, Acryllatices, Polybutadien, Polyisopren und Polybuten.
  10. Verfahren zur Herstellung einer thermoplastischen Formmasse, welches umfaßt das Mischen :
    A. von 5 bis 95 Gew.-% eines aromatischen Polycarbonates;
    B. von 60 bis 2 Gew.-% eines aromatischen Polyesters; und
    C. von 0,1 bis 40 Gew.-% eines Copolymeren von Ethylen und Kohlenmonoxid, wobei dieses Copolymere kenn Terpolymeres oder höheres Polymeres ist, und es von 0,1 bis 50 Gew.-% Kohlenmonoxid umfaßt,
    und anschließend das Schmelzmischen von A, B und C.
EP89120488A 1988-11-07 1989-11-06 Thermoplastische Formmasse und Verfahren zu deren Herstellung Expired - Lifetime EP0368198B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US268104 1988-11-07
US07/268,104 US4859738A (en) 1988-11-07 1988-11-07 Environmental stress failure resistant polycarbonate blend

Publications (3)

Publication Number Publication Date
EP0368198A2 EP0368198A2 (de) 1990-05-16
EP0368198A3 EP0368198A3 (de) 1991-07-10
EP0368198B1 true EP0368198B1 (de) 1995-06-07

Family

ID=23021496

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89120488A Expired - Lifetime EP0368198B1 (de) 1988-11-07 1989-11-06 Thermoplastische Formmasse und Verfahren zu deren Herstellung

Country Status (9)

Country Link
US (1) US4859738A (de)
EP (1) EP0368198B1 (de)
JP (1) JPH0689244B2 (de)
KR (1) KR900007954A (de)
AT (1) ATE123514T1 (de)
AU (1) AU626603B2 (de)
CA (1) CA2002258A1 (de)
DE (1) DE68922962T2 (de)
MX (1) MX165309B (de)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4894423A (en) * 1988-11-07 1990-01-16 The Dow Chemical Company Environmental stress failure resistant polycarbonate
US5242981A (en) * 1989-01-26 1993-09-07 Kawasaki Steel Corporation Resin composition
US5189091A (en) * 1989-05-04 1993-02-23 The Dow Chemical Company Polycarbonate/aromatic polyester blends modified with a grafted olefin copolymer
US5278694A (en) * 1990-01-11 1994-01-11 The Dow Chemical Company Optically dissimilar composition for polymeric reflective bodies
US5308894A (en) * 1990-04-12 1994-05-03 The Dow Chemical Company Polycarbonate/aromatic polyester blends containing an olefinic modifier
US5369154A (en) * 1990-04-12 1994-11-29 The Dow Chemical Company Polycarbonate/aromatic polyester blends containing an olefinic modifier
US5132360A (en) * 1990-05-29 1992-07-21 Shell Oil Company Polyketone polymer blends
US5124402A (en) * 1990-08-21 1992-06-23 The Dow Chemical Company Thermoplastic molding compositions with improved solvent resistance and impact strength, and methods for preparation thereof
US5082890A (en) * 1990-08-21 1992-01-21 The Dow Chemical Company Filled thermoplastic molding compositions
US5300350A (en) * 1993-02-22 1994-04-05 The Dow Chemical Company Black-colored, laser-writable blends of carbonate polymer and polyester
KR100553535B1 (ko) * 2004-10-27 2006-02-21 제일모직주식회사 내화학성이 우수한 폴리카보네이트계 수지 조성물

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248359A (en) * 1961-04-27 1966-04-26 Du Pont Polyolefin compositions
US3431224A (en) * 1962-07-11 1969-03-04 Gen Electric Polycarbonate resin mixtures

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT293013B (de) * 1968-04-25 1971-09-27 Bayer Ag Verfahren zur Herstellung von Segmentcopolymerisaten aus 1,3-Dienen und vinylaromatischen Verbindungen
US4076911A (en) * 1975-11-05 1978-02-28 Union Oil Company Of California Ethylene-carbon monoxide copolymers
US4180494A (en) * 1977-08-15 1979-12-25 Rohm And Haas Company Thermoplastic polyesters
US4271063A (en) * 1978-12-26 1981-06-02 General Electric Company Thermoplastic molding compositions
DE3002662A1 (de) * 1980-01-25 1981-07-30 Bayer Ag, 5090 Leverkusen Flammwidrige thermoplastische formmassen aus polycarbonaten und abs-polymerisaten
US4639481A (en) * 1982-09-27 1987-01-27 General Electric Company Modified thermoplastic polyester molding compositions and articles molded therefrom
US4520164A (en) * 1982-12-22 1985-05-28 General Electric Company Blends of aromatic polycarbonate resins, polyolefins and olefin copolymers, and acrylate interpolymer resins
US4476274A (en) * 1983-01-03 1984-10-09 General Electric Company Linear low density polyethylene impact modifier for thermoplastic polyesters
US4536542A (en) * 1983-11-18 1985-08-20 General Electric Company Method for altering the surface of thermoplastic polymers
US4894423A (en) * 1988-11-07 1990-01-16 The Dow Chemical Company Environmental stress failure resistant polycarbonate

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3248359A (en) * 1961-04-27 1966-04-26 Du Pont Polyolefin compositions
US3431224A (en) * 1962-07-11 1969-03-04 Gen Electric Polycarbonate resin mixtures

Also Published As

Publication number Publication date
ATE123514T1 (de) 1995-06-15
AU626603B2 (en) 1992-08-06
KR900007954A (ko) 1990-06-02
JPH02182754A (ja) 1990-07-17
EP0368198A2 (de) 1990-05-16
EP0368198A3 (de) 1991-07-10
MX165309B (es) 1992-11-04
DE68922962T2 (de) 1995-10-19
US4859738A (en) 1989-08-22
DE68922962D1 (de) 1995-07-13
JPH0689244B2 (ja) 1994-11-09
AU4445489A (en) 1990-05-10
CA2002258A1 (en) 1990-05-07

Similar Documents

Publication Publication Date Title
US3334154A (en) Flame retardant mixed polycarbonate resins prepared from tetrabromo bisphenol-a
US5674928A (en) Thermoplastic resin compositions containing a high hydroxyl polyester and a polycarbonate, and articles made therefrom
US5124402A (en) Thermoplastic molding compositions with improved solvent resistance and impact strength, and methods for preparation thereof
EP0368198B1 (de) Thermoplastische Formmasse und Verfahren zu deren Herstellung
JPS63501428A (ja) ポリカ−ボネ−ト組成物
US3269971A (en) Polycarbonate flow extenders
JP3466787B2 (ja) ビスクロルホルメート法による共ポリエステルカーボネートの製造法
EP0368197B1 (de) Thermoplastische Formmasse und Verfahren zu deren Herstellung
JP3899178B2 (ja) 難燃性樹脂組成物
GB1569230A (en) Flame retardant compositions comprising block copolyesters of polybutylene terephthalate
EP0525051B1 (de) Olefinisches modifizierungsmittel enthaltende mischungen von polykarbonat und aromatischem polyester
WO1992014787A1 (en) Blends of thermoplastic molding compositions containing epoxy resins
EP0363885A2 (de) Polycarbonat-Mischung und Verfahren zu ihrer Herstellung
JP4080578B2 (ja) ガラス転位温度の低い難燃性ポリエステルカーボネート
US4929676A (en) Impact and chemical resistant polycarbonate blend
JP3495197B2 (ja) 熱可塑性樹脂組成物
US3897391A (en) Process for preparing polycarbonate
US5082890A (en) Filled thermoplastic molding compositions
US5414046A (en) Flame retardant polymer compositions comprising thermally stable resins
US4563503A (en) Polycarbonate compositions having improved impact performance
US4448950A (en) Polycarbonate having improved critical thickness
US4425456A (en) Copolycarbonates based on bis(4-hydroxyphenyl)biphenyl disulfone
JPH05194843A (ja) 樹脂組成物
CA1131837A (en) Composition of a polycarbonate resin and a selectively hydrogenated block copolymer of a vinyl aromatic compound and an olefinic elastomer
JPH0114938B2 (de)

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH DE FR GB IT LI NL SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): AT BE CH DE FR GB IT LI NL SE

17P Request for examination filed

Effective date: 19911218

17Q First examination report despatched

Effective date: 19940222

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE FR GB IT LI NL SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19950607

Ref country code: LI

Effective date: 19950607

Ref country code: CH

Effective date: 19950607

Ref country code: BE

Effective date: 19950607

Ref country code: AT

Effective date: 19950607

REF Corresponds to:

Ref document number: 123514

Country of ref document: AT

Date of ref document: 19950615

Kind code of ref document: T

ET Fr: translation filed
REF Corresponds to:

Ref document number: 68922962

Country of ref document: DE

Date of ref document: 19950713

ITF It: translation for a ep patent filed

Owner name: ING. A. GIAMBROCONO & C. S.R.L.

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19950907

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19951106

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19951106

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Effective date: 19960731

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Effective date: 19960801

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20051106